학술논문

An epithelial to mesenchymal transition programme does not usually drive the phenotype of invasive lobular carcinomas
Document Type
Report
Source
Journal of Pathology. March, 2016, Vol. 238 Issue 4, p489, 6 p.
Subject
Cancer -- Genetic aspects
Cancer -- Development and progression
Cancer -- Analysis
Intermediate filament proteins -- Analysis
Immunohistochemistry -- Analysis
Muscle proteins -- Analysis
Stem cells -- Analysis
Gene expression -- Analysis
Fibronectins -- Analysis
Health
Language
English
ISSN
0022-3417
Abstract
Byline: , , Ana C Vargas, Janani Jayanthan, Amel Al-Murrani, Lynne E Reid, Rachael Chambers, Leonard Da Silva, Lewis Melville, Elizabeth Evans, Alan Porter, David Papadimos, Erik W Thompson, Sunil R Lakhani, Peter T Simpson Keywords: breast cancer; invasive lobular carcinoma; epithelial to mesenchymal transition (EMT); E-cadherin Abstract Epithelial to mesenchymal transition (EMT) is a cellular phenotype switching phenomenon which occurs during normal development and is proposed to promote tumour cell invasive capabilities during tumour progression. Invasive lobular carcinoma (ILC) is a histological special type of breast cancer with a peculiar aetiology - the tumour cells display an invasive growth pattern, with detached, single cells or single files of cells, and a canonical feature is the loss of E-cadherin expression. These characteristics are indicative of an EMT or at the very least that they represent some plasticity between phenotypes. While some gene expression profiling data support this view, the tumour cells remain epithelial and limited immunohistochemistry data suggest that EMT markers may not feature prominently in ILC. We assessed the expression of a panel of EMT markers (fibronectin, vimentin, N-cadherin, smooth muscle actin, osteonectin, Snail, Twist) in 148 ILCs and performed a meta-analysis of publically available molecular data from 154 ILCs. Three out of 148 (2%) ILCs demonstrated an early and coordinated alteration of multiple EMT markers (down-regulation of E-cadherin, nuclear TWIST, and up-regulation of vimentin, osteonectin, and smooth muscle actin). However, the data overall do not support a role for EMT in defining the phenotypic peculiarities of the majority of ILCs. Copyright [c] 2015 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd. Article Note: These authors made an equal contribution No conflicts of interest were declared CAPTION(S): FigureS1 Whole section, with higher power inset of the ILC case presented in Figure 1. FigureS2 Low-power whole section, with higher power inset of the second EMT-positive ILC case shown in Figure 1. FigureS3 Low-power whole section, with higher power inset of the third EMT-positive ILC case.